NCBI
dbSNP
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This legacy RefSNP page contains old data from dbSNP build 151 (March 2018) and is no longer maintained. Please update your links and bookmarks to use the re-designed RefSNP Report page.
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Reference SNP (refSNP) Cluster Report: rs866348371                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:147/151
Map to Genome Build:108/Weight 1
Validation Status:byCluster
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:G/T (FWD)
Allele Origin:
Ancestral Allele:Not available
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:G=0.1644/20645 (TOPMED)
HGVS Names
  • CM000663.2:g.136635T>G
  • NC_000001.10:g.136635T>G
  • NC_000001.11:g.136635T>G
  • NR_039983.2:n.3612A>C
Links
SNP Details are organized in the following sections:
GeneView Map Submission Fasta Resource Diversity Validation

  Integrated Maps (Hint: click on 'Chr Pos' to see variant in the new NCBI variation viewer) back to top

  GeneView back to top

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Submitter records for this RefSNP Cluster back to top
The submission ss1917958764 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs866348371 during BLAST analysis for the current build.


NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss1917958764WEILL_CORNELL_DGM|SNV:chr1:136635fwd/BG/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc10/16/1510/16/15147Genomicunknown
ss1997003431TMC_SNPDB|chr1136635TGfwd/BG/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc05/19/1605/19/16147Genomicunknown
ss2147483751USC_VALOUEV|NC_000001.10:g.136635T>Gfwd/G/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc11/17/1611/17/16150Genomicunknown
ss2697373311GRF|SNV2079939fwd/G/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc02/13/1702/13/17151Genomicunknown
ss2750611426GNOMAD|rs866348371fwd/G/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc05/17/1705/17/17151Genomicunknown
ss2986143444SWEGEN|NC_000001.10:g.136635T>Gfwd/G/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc05/30/1705/30/17151Genomicunknown
ss3343271745CSHL|LID=SNVhg19:chr1:136635fwd/G/Tcctctgtccgcgtgggaggggccgggtgaggcaaggggctcaggctgacc10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs866348371|allelePos=26|totalLen=51|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=151
 CCTCTGTCCG CGTGGGAGGG GCCGG
 K
 GTGAGGCAAG GGGCTCAGGC TGACC

  NCBI Resource Links back to top
Submitter-Referenced
dbSNP Blast Analysis

  Population Diversity (Alleles in RefSNP orientation) back to top
There is no frequency data.

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterUNKNOWNUNKNOWNUNKNOWN